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Determination of correct zeta potential of polyether sulfone membranes using CLC and AGC: ionic environment effect

机译:使用CLC和AGC测定聚醚砜膜的正确Zeta电位:离子环境效应

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摘要

In this study, the correct and apparent zeta potential of polyether sulfone (PES) ultrafiltration membranes at different ionic environments were determined using streaming potential measurements. The apparent zeta potential was found by calculation with classic Helmholtz-Smoluchowski (HS) and Fairbrother-Mastin (FM) equations of results obtained from clamping cell (CLC) and adjustable gap cell (AGC). Correct zeta potential was determined by calculation with a modified HS equation of obtained results from AGC. Obtained apparent zeta potential results from CLC and AGC differ from each other, and the reproducibilityof results was found to be higher for measurements of AGC. Except for low pH values, apparent zeta potential that was obtained from classic HS equation with AGC could be accepted as correct zeta potential. In CLC measurements, underestimated or overestimated zeta potential values were determined in comparison with the correct zeta potential. The effect of membrane surface conductance on zeta potential decreased with increasing KCl concentration. In CLC, the deviation was observed from electrical double layer theory when KCl concentration was 0.1M, therefore streaming potential measurements did not produce correct results at higher salt concentration. 0.001M KCl concentration was the value at which surface conductance became crucial.
机译:在该研究中,使用流电位测量确定在不同离子环境下的聚醚砜(PES)超滤膜的正确和表观Zeta电位。通过使用经典的Helmholtz-Smoluchowski(HS)和Fairbrother-Mastin(FM)方程来发现表观Zeta电位,从夹紧电池(CLC)和可调节的间隙细胞(AGC)获得的结果。通过用来自AGC的获得结果的改进的HS方程计算确定正确的Zeta电位。从CLC和AGC获得的明显Zeta电位均相彼此不同,结果的再现性较高,用于测量AGC。除了低pH值外,从经典HS方程获得的表观Zeta电位可以接受为正确的Zeta电位。在CLC测量中,与正确的Zeta电位相比,确定低估或高估的Zeta电位值。随着KCl浓度的增加,膜表面电导对Zeta电位的影响降低。在CLC中,当KCl浓度为0.1M时,从电双层理论观察到偏差,因此流势势测量不会以较高的盐浓度产生正确的结果。 0.001M KCl浓度是表面电导变得至关重要的值。

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